Suppr超能文献

全血样本基因表达谱中珠蛋白RNA干扰的特征分析。

Characterization of globin RNA interference in gene expression profiling of whole-blood samples.

作者信息

Wright Christopher, Bergstrom Donald, Dai Hongyue, Marton Matthew, Morris Mark, Tokiwa George, Wang Yanqun, Fare Thomas

机构信息

Rosetta Inpharmatics, Merck & Co., Inc., Seattle, WA 98109, USA.

出版信息

Clin Chem. 2008 Feb;54(2):396-405. doi: 10.1373/clinchem.2007.093419. Epub 2007 Dec 18.

Abstract

BACKGROUND

Blood-based biomarker discovery with gene expression profiling has been hampered by interference from endogenous, highly abundant alpha- and beta-globin transcripts. We describe a means to quantify the interference of globin transcripts on profiling and the effectiveness of globin transcript mitigation by (a) defining and characterizing globin interference, (b) reproducing globin interference with synthetic transcripts, and (c) using ROC curves to measure sensitivity and specificity for a protocol for removing alpha- and beta-globin transcripts.

METHODS

We collected blood at 2 sites and extracted total RNA in PreAnalytiX PAXgene tubes. As a reference for characterizing interference, we supplemented aliquots of total RNA with synthesized globin transcripts and total RNA from human brain. Selected aliquots were processed with Ambion GLOBINclear to remove globin transcripts. All aliquots were labeled and hybridized to Agilent DNA microarrays by means of pooling schemes designed to quantify the mitigation of globin interference and to titrate gene expression signatures. Quantitative reverse transcription-PCR data were generated for comparison with microarray results.

RESULTS

Our supplementation and pooling strategy for comparing the microarray data among samples demonstrated that mitigation could reduce an interference signature of >1000 genes to approximately 200. Analysis of samples of endogenous globin transcripts supplemented with brain RNA indicated that results obtained with the GLOBINclear treatment approach those of peripheral blood mononuclear cell preparations.

CONCLUSION

We confirmed that both the absolute concentrations of globin transcripts and differences in transcript concentrations within a sample set are factors that cause globin interference (Genes Immun 2005;6:588-95). The methods and transcripts we have developed may be useful for quantitatively characterizing globin mRNA interference and its mitigation.

摘要

背景

基于基因表达谱的血液生物标志物发现受到内源性、高丰度的α-和β-珠蛋白转录本的干扰。我们描述了一种方法,通过(a)定义和表征珠蛋白干扰,(b)用合成转录本重现珠蛋白干扰,以及(c)使用ROC曲线测量去除α-和β-珠蛋白转录本方案的敏感性和特异性,来量化珠蛋白转录本对谱分析的干扰以及珠蛋白转录本缓解的有效性。

方法

我们在2个地点采集血液,并在PreAnalytiX PAXgene管中提取总RNA。作为表征干扰的参考,我们用合成的珠蛋白转录本和来自人脑的总RNA补充总RNA的等分试样。选定的等分试样用Ambion GLOBINclear处理以去除珠蛋白转录本。所有等分试样都进行标记,并通过旨在量化珠蛋白干扰缓解和滴定基因表达特征的合并方案与安捷伦DNA微阵列杂交。生成定量逆转录-PCR数据以与微阵列结果进行比较。

结果

我们用于比较样品间微阵列数据的补充和合并策略表明,缓解可将>1000个基因的干扰特征减少到约200个。对内源性珠蛋白转录本补充脑RNA的样品分析表明,GLOBINclear处理方法获得的结果与外周血单核细胞制备的结果相当。

结论

我们证实,珠蛋白转录本的绝对浓度和样品组内转录本浓度的差异都是导致珠蛋白干扰的因素(《基因与免疫》2005年;6:588 - 95)。我们开发的方法和转录本可能有助于定量表征珠蛋白mRNA干扰及其缓解情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验